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CAS 380430-58-0

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[4-(E-3-Methoxy-3-oxo-1-propen-1-yl)phenyl]boronic acid

Description:
[4-(E-3-Methoxy-3-oxo-1-propen-1-yl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a propenyl group that contains a methoxy and a ketone functional group, contributing to its reactivity and potential applications in organic synthesis and medicinal chemistry. The boronic acid moiety allows for participation in Suzuki coupling reactions, making it valuable in the formation of carbon-carbon bonds. Additionally, the presence of the methoxy and keto groups can influence the compound's solubility, stability, and biological activity. Typically, boronic acids are sensitive to moisture and can undergo hydrolysis, which may affect their handling and storage. Overall, this compound's unique structure and functional groups position it as a versatile intermediate in various chemical reactions and applications in drug development and materials science.
Formula:C10H11BO4
InChI:InChI=1/C10H11BO4/c1-15-10(12)7-4-8-2-5-9(6-3-8)11(13)14/h2-7,13-14H,1H3/b7-4+
InChI key:InChIKey=BIKAXBPCHWDATP-QPJJXVBHSA-N
SMILES:C(=C/C(OC)=O)\C1=CC=C(B(O)O)C=C1
Synonyms:
  • 1-Methyl (2E)-3-(4-boronophenyl)-2-propenoate
  • 2-Propenoic acid, 3-(4-boronophenyl)-, 1-methyl ester, (2E)-
  • {4-[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]phenyl}boronic acid
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